Evidence map›Paper›PMID 16904662›Full record

ArticleDevelopmental biology2006

Differential gene expression and functional analysis implicate novel mechanisms in enteric nervous system precursor migration and neuritogenesis.

Bhupinder P S Vohra, Keiji Tsuji, Mayumi Nagashimada, Toshihiro Uesaka, Daniel Wind, Ming Fu, Jennifer Armon, Hideki Enomoto, Robert O Heuckeroth

Open access · greenAbstract read
In one paragraph

Article in Developmental biology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
4.6field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 67 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 2 countries.

Bhupinder P S VohraDepartment of Pediatrics, Washington University School of Medicine, St. Louis, MO 63110, USA.
Keiji Tsuji
Mayumi Nagashimada
Toshihiro Uesaka
Daniel Wind
Ming Fu
Jennifer Armon
Hideki Enomoto
Robert O Heuckeroth
Washington University in St. Louis · USKyoto Prefectural University of Medicine · JPThe University of Osaka · JP

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI TIMOTHY J. EBERLEIN · 2001 to 2026
$128.0M
Neuronal control of intestinal motility in mutant miceR01DK064592 · NIDDK · WASHINGTON UNIVERSITY · PI HEUCKEROTH, ROBERT O · 2003 to 2007
$2.5M
RET LIGAND REGULATION OF INTESTINAL MOTILITYR01DK057038 · NIDDK · WASHINGTON UNIVERSITY · PI HEUCKEROTH, ROBERT O · 2000 to 2009
$2.0M
Activin vs BMP Signaling in Pancreatic Lineage SelectionR01DK064952 · NIDDK · CHILDREN'S MERCY HOSP (KANSAS CITY, MO) · PI GITTES, GEORGE K. · 2004 to 2008
$1.6M
Proteomics of Biliary AtresiaR21DK068371 · NIDDK · WASHINGTON UNIVERSITY · PI HEUCKEROTH, ROBERT O · 2004 to 2005
$306k
NCI NIH HHS P30 CA091842NCI NIH HHS P30 CA91842NIDDK NIH HHS DK057038NIDDK NIH HHS DK068371NIDDK NIH HHS DK64952NIDDK NIH HHS R01 DK057038NIDDK NIH HHS R01 DK064592NIDDK NIH HHS R21 DK068371
6 · The paper itself

Abstract

Enteric nervous system (ENS) development requires complex interactions between migrating neural-crest-derived cells and the intestinal microenvironment. Although some molecules influencing ENS development are known, many aspects remain poorly understood. To identify additional molecules critical for ENS development, we used DNA microarray, quantitative real-time PCR and in situ hybridization to compare gene expression in E14 and P0 aganglionic or wild type mouse intestine. Eighty-three genes were identified with at least two-fold higher expression in wild type than aganglionic bowel. ENS expression was verified for 39 of 42 selected genes by in situ hybridization. Additionally, nine identified genes had higher levels in aganglionic bowel than in WT animals suggesting that intestinal innervation may influence gene expression in adjacent cells. Strikingly, many synaptic function genes were expressed at E14, a time when the ENS is not needed for survival. To test for developmental roles for these genes, we used pharmacologic inhibitors of Snap25 or vesicle-associated membrane protein (VAMP)/synaptobrevin and found reduced neural-crest-derived cell migration and decreased neurite extension from ENS precursors. These results provide an extensive set of ENS biomarkers, demonstrate a role for SNARE proteins in ENS development and highlight additional candidate genes that could modify Hirschsprung's disease penetrance.

Indexed as

Cell Movementalpha CateninAnimalsCadherin Related ProteinsCadherinsCells, CulturedChromosome PairingEnteric Nervous SystemEpitheliumGene ExpressionHirschsprung DiseaseIntestinal MucosaMiceMice, Inbred C57BLMice, KnockoutMorphogenesisalpha CateninCadherin Related ProteinsCadherinsCDHR15 protein, mouseProtein PrecursorsProto-Oncogene Proteins c-retRet protein, mouseSNARE Proteins

Identifiers

PMID16904662
PMCPMC1952185
OpenAlexW2085901785

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.